HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Carbethoxycarbonylmethyl-2-amino-3-carbamoyl-quinoxalinium bromide → Ethyl 4-carbamoyl-imidazo-[1,2-a]-quinoxaline-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Carbethoxycarbonylmethyl-2-amino-3-carbamoyl-quinoxalinium bromide | HCID 20287983 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-carbamoyl-imidazo-[1,2-a]-quinoxaline-2-carboxylate | HCID 14067521 | 74.1% |
Reaction Steps
A suspension of 1 g of the product of Step A in 100 ml of ethanol was refluxed with stirring for 90 minutes and the resulting yellow solution was concentrated and cooled. The mixture was filtered to obtain 0.55 g of ethyl 4-carbamoyl-imidazo-[1,2-a]-quinoxaline-2-carboxylate as a pale yellow crystalline solid. Recrystallization from ethanol yielded soft white needles melting at 280°-284° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04254123 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-f314d70b542d41eeba794cd016ca4891 |
| Source note | uspto-grants-1981_03 |